| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4169615 | The Journal of Pediatrics | 2006 | 4 Pages |
Abstract
Our findings indicate that the father provided consistent haplotypes leading to the expression of SCN in all affected children, supporting an autosomal dominant inheritance in which ELA2 mutations occur.
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Perinatology, Pediatrics and Child Health
Authors
Laurence A. MD, Steven BA, Danielle PhD, Audrey Anna BA, David C. MD,